gudid
Primary ID: 1.002.7000
DIAGNOdent pen 2190 (UDI 1.002.7000)
Manufactured by KaVo Dental GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DIAGNOdent pen 2190 - Primary ID 1.002.7000
Device Regulatory Overview
The DIAGNOdent pen 2190 (Model/Catalog Number: 1.002.7000) is a medical device manufactured by KaVo Dental GmbH. This product is indexed under FDA Product Code / Category Classification NTK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1.002.7000
- Product Code / EMDN
- NTK
- Device Name
- This is a medical device.
- Database Sync Date
- 2026-08-09 09:08:27
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of DIAGNOdent pen 2190?
The registered manufacturer of record for DIAGNOdent pen 2190 is KaVo Dental GmbH.
What is the Primary UDI-DI identifier for DIAGNOdent pen 2190?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.002.7000.
What classification code is assigned to this device?
This device is registered under product classification code NTK.
Similar Classification Devices (NTK)
Other Devices by KaVo Dental GmbH
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